WO2017222965A1 - Synergistic combination of biocides - Google Patents
Synergistic combination of biocides Download PDFInfo
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- WO2017222965A1 WO2017222965A1 PCT/US2017/038101 US2017038101W WO2017222965A1 WO 2017222965 A1 WO2017222965 A1 WO 2017222965A1 US 2017038101 W US2017038101 W US 2017038101W WO 2017222965 A1 WO2017222965 A1 WO 2017222965A1
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/02—Local antiseptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- a disinfectant refers to any chemical agent capable of killing, destroying, or inhibiting the growth of organisms, particularly microorganisms.
- Disinfectant products include hard surface cleaners, hand sanitizers, pre-disinfectant cleaners for instruments, sterilizing and high-level disinfectant compositions, and the like.
- a disinfectant has broad-spectrum activity against all types of microorganisms at various pH levels.
- the disinfectant should also have high efficacy so that a minimum amount of the anti-microbial agent can be used to save cost and to avoid or reduce any possible adverse effects caused by the antimicrobial agent.
- it is desirable that the disinfectant is stable to any changes in temperature encountered during manufacturing, packaging, and shipping as well as during storage.
- an ideal disinfectant is physically and chemically compatible with ingredients of different application systems so that the antimicrobial agent can suitably be incorporated in various products.
- disinfectants that have been used in the past include alcohols such as isopropyl alcohol and ethanol, copper compounds, silver compounds, aldehydes, oxidizing agents such as sodium hypochlorite, and the like.
- quaternary compounds have also been used in the past. Quaternary compounds, however, can have a limited activity spectrum. In addition, in certain applications, quaternary compounds need to be used at relatively high concentrations in order to achieve desired efficacy. Adding relatively high concentrations of a quaternary compound to a product, however, can be problematic. For instance, not only is the quaternary compound expensive to manufacture and produce but can also be subject to various regulatory requirements. Consequently, a need exists for a method for increasing the efficacy spectrum of quaternary compounds and simultaneously reducing the required concentration of the compounds while still maintaining the desired effect. In this regard, the present disclosure is directed to improved anti-microbial compositions containing a quaternary compound and to methods for using the compositions.
- an anti-microbial composition contains a first biocide in combination with a second biocide.
- the first biocide comprises a salt of a quaternary ammonium cation.
- the first biocide may comprise a carbonate/bicarbonate, halide, or propionate salt of a quaternary ammonium cation.
- the second biocide is selected depending on the particular biocide properties desired such that the second biocide synergistically operates in conjunction with the first biocide in order to kill or inhibit the growth of a microorganism or a plurality of different microorganisms.
- a synergistic interaction refers to the fact that the two biocides combined together have a total effect that is greater than the biocide properties of only one of the biocides acting alone.
- the first and second biocides of the present disclosure operate synergistically together so as to have greater antimicrobial activity in the presence of each against a certain microorganism than in comparison to the antimicrobial activity of the first biocide alone or the
- the amount of the first biocide present in the composition can be reduced while still producing the desired efficacy.
- the present disclosure is directed to a composition having biocidal properties that comprises a first biocide comprising a salt of a quaternary ammonium cation and a second biocide selected so as to
- the second biocide can comprise a biguanide.
- the second biocide is present in the composition in relation to the first biocide such that the ability of both biocides to kill or inhibit the growth of the microorganism is greater than if only one of the biocides were present at the same concentration of both biocides together.
- the antimicrobial composition of the present disclosure can control gram positive bacteria, gram negative bacteria, fungi, yeast, spores, viruses, and the like. Examples of particular microorganisms that may be controlled in accordance with the present disclosure include Escherichia coli, Staphylococcus aureus, Aspergillus brasiliensis, or mixtures thereof.
- the second biocide may comprise a biguanide and derivatives thereof.
- the second biocide may comprise polyhexamethylene biguanide or chlorhexidine gluconate.
- the first biocide and the second biocide may be present in the composition at a weight ratio of from about 1 :20 to about 20: 1 , such as from about 1 :5 to about 5: 1 .
- the anti-microbial composition of the present disclosure can be used in numerous and different products.
- the anti-microbial composition can be incorporated into a hard surface cleaner, a hand sanitizer, a disinfectant solution for instruments such as medical instruments, or in any other suitable disinfectant product.
- the anti-microbial composition of the present disclosure can also be used as a preservative composition and may be contained, for instance, in a cosmetic or hygiene product.
- the cosmetic or hygiene product may comprise a base composition and a preservative, wherein the preservative comprises the combination of biocides as described above.
- the present disclosure is also directed to a method for producing a disinfectant composition.
- the method includes combining a first biocide
- the second biocide can be a biguanide or any salts, analogs, or derivatives thereof.
- the present disclosure is directed to a composition having biocidal properties.
- the composition has numerous uses and applications.
- the composition may comprise a disinfectant.
- the disinfectant can be used in any suitable industry or field.
- the disinfectant can be used in the food and beverage field, may comprise an institutional product, a domestic product, or a healthcare product.
- the disinfectant for instance, may comprise a hard surface disinfectant, a hand sanitizer, a sterilizing or high-level disinfectant composition, a pre-disinfectant cleaner for instruments, and the like.
- the composition may be used as a preservative for a product, such as a personal care product or a hygiene product.
- the composition of the present disclosure contains a first biocide that comprises a salt of a quaternary ammonium cation.
- the first biocide may comprise a carbonate/bicarbonate, halide, or propionate salt of a quaternary ammonium cation.
- the first biocide is combined with a second biocide to kill and/or control one or more microorganisms.
- the first biocide and the second biocide in accordance with the present disclosure operate synergistically together in order to kill or inhibit the growth of the microorganism. More particularly, the two biocides combined together in accordance with the present disclosure have greater efficacy at a lower concentration than if one of the biocides were present alone in the composition.
- the use of two different biocides also can enhance the spectrum of activity of the composition against multiple microorganisms.
- the anti-microbial infections are examples of the anti-microbial activity of the composition against multiple microorganisms.
- composition of the present disclosure can be used at lower concentrations and yet be more effective against a wider range of microorganisms.
- Selection of the second biocide to be used in conjunction with the first biocide can be based upon the target microorganism and can be selected using a screening procedure.
- an anti-microbial composition can be produced with a total
- the present disclosure includes at least a first biocide and a second biocide.
- a third biocide and/or a fourth biocide may be present to further enhance the synergistic effects.
- the first biocide generally comprises a quaternary ammonium salt. Consequently, the present disclosure, in one embodiment, is directed particularly to selecting a second biocide that has synergistic interactions with a quaternary ammonium salt. In this manner, the amount of quaternary ammonium salt contained in the composition can be minimized. In addition, due to the synergistic interactions, the amount of the second biocide can also be minimized.
- compositions can be made according to the present disclosure that contain two biocides having synergistic interactions wherein both biocides are contained in the composition at a total concentration less than if only one or more quaternary ammonium salts were present in the composition while still having the same or better efficacy against one or more target microorganisms.
- the first biocide may comprise a quaternary ammonium carbonate.
- a quaternary ammonium carbonate can be represented by the following formula:
- R 1 is a C1-C20 alkyl or aryl-substituted alkyl group and R 2 is a C 8 -C 2 o alkyl group, and preferably wherein R 1 is the same as R 2 and R 1 is a C8-C12 alkyl group, as well as compositions further comprising the corresponding quaternary ammonium bicarbonate
- R 1 is the same or a different C1-C20 alkyl or aryl-substituted alkyl group as above and R 2 is the same or a different C8-C20 alkyl group as above, but preferably wherein R 1 is the same as R 2 and R 1 is a C8-C12 alkyl group.
- the first biocide contained in the composition comprises a di C8-C12 alkyl ammonium carbonate/bicarbonate.
- the antimicrobial or preservative composition contains didecyl dimethyl ammonium carbonate and didecyl dimethyl ammonium
- the carbonate/bicarbonate salts of quaternary ammonium cations may be selected from dioctyldimethylammonium carbonate, decyloctyldimethylammonium carbonate, benzalkonium carbonate, benzethonium carbonate, stearalkonium carbonate, cetrimonium carbonate, behentrimonium carbonate, dioctyldimethylammonium bicarbonate,
- decyloctyldimethylammonium bicarbonate benzalkonium bicarbonate
- benzethonium bicarbonate stearalkonium bicarbonate, cetrimonium bicarbonate, behentrimonium bicarbonate, and mixtures of one or more such carbonate salts.
- the first biocide may comprise a quaternary ammonium halide.
- the quaternary ammonium halide may comprise, for instance, an alkyl quaternary ammonium halide or a benzyl ammonium halide.
- Quaternary ammonium compounds also known as “quats”, typically comprise at least one quaternary ammonium cation with an appropriate anion. Quats will generally have the general formula (1 ).
- R-i , R 2 , R3 and R 4 can vary within wide limits and examples of quaternary ammonium compounds that have anti-microbial properties will be well known to the person of ordinary skill in the art.
- two of R-i, R 2 , R3 and R 4 are lower alkyl, meaning having 1 to 4 carbon atoms, such as methyl, ethyl, propyl or butyl groups.
- two of R-i, R 2 , R3 and R 4 are longer chain alkyl groups of 6 to 24 carbon atoms, or a benzyl group.
- a " is a monovalent anion or one equivalent of a polyvalent anion of an inorganic or organic acid.
- Suitable anions for A " are in principle all inorganic or organic anions, in particular halides, for example chloride or bromide, carboxylates, sulfonates, phosphates or a mixture thereof.
- the quaternary ammonium compound may comprise a dialkyl ammonium compound, such as a dimethyl dialkyl ammonium compound.
- the dimethyl dialkyl ammonium compound may have between about 8 and about 12 carbon atoms, such as from about 8 to about 10 carbon atoms in each of the alkyl groups.
- dimethyl dialkyl ammonium compounds which may be used as the first biocide include dimethyl dioctyl ammonium compounds such as dimethyl dioctyl ammonium chloride, dimethyl didecyl ammonium compounds such as dimethyl didecyl ammonium chloride and the like. Mixtures of dimethyl dialkyl ammonium compounds may also be used, and other anions, such as those described above, may also be used.
- Commercially available dimethyl dialkyl ammonium compounds include, for example, compositions marketed and sold under the BARDACTM tradename by Lonza America, Inc.
- the first biocide may comprise a benzyl ammonium compound, such as an alkyl dimethyl benzyl ammonium compound.
- the alkyl group may contain from about 10 to about 18 carbon atoms, such as from about 12 to about 16 carbon atoms.
- alkyl dimethyl benzyl ammonium compounds useable as the first biocide include C12 alkyl dimethyl benzyl ammonium chloride, Ci 4 alkyl dimethyl benzyl ammonium chloride, and C16 alkyl dimethyl benzyl ammonium chloride. In addition, a mixture of these alkyl dimethyl benzyl ammonium compounds can be used.
- Commercially available alkyl dimethyl benzyl ammonium compounds include, for example, compositions marketed and sold under the BARQUAT ® tradename by Lonza America, Inc.
- the first biocide as described above is combined with at least a second biocide in accordance with the present disclosure.
- a second biocide is selected that synergistically operates with the first biocide to destroy and/or inhibit the growth of a target microorganism or a plurality of target microorganisms.
- a second biocide is selected that is capable of increasing the efficacy of the first biocide against a microorganism such that the overall concentration of biocides in the composition can be reduced in comparison to a composition that only contains one of the biocides.
- the second biocide can be selected through a screening process to determine synergistic interactions.
- the second biocide may comprise various different compounds depending upon the particular application and the microorganisms that are to be controlled.
- R 1 , R 2 , R 3 and R 4 are each independently chosen from hydrogen, optionally substituted alkyl, optionally substituted phenyl, ethylene glycol, diethylene glycol, methylene glycol and tetraethylene glycol, or one of R 1 , R 2 , R 3 and R 4 may be
- the second biocide may comprise a polyalkylene biguanide, such as polyhexamethylene biguanide.
- the second biocide may comprise polyhexamethylene biguanide hydrochloride (PHMB), also known as polyaminopropyl biguanide (PABP).
- PHMB polyhexamethylene biguanide hydrochloride
- PABP polyaminopropyl biguanide
- PHMB is commonly represented by the following formula, though it is known to exist as a complex mixture of polymeric biguanides with various terminal groups including guanidine (not shown).
- n represents the number of repeating units of the biguanide polymer.
- PHMB can be a mixture of various biguanide polymers that can include different combinations of terminal groups, e.g., amine,
- PHMB-AA biguanide polymer with two terminal amine groups
- PHMB-CGCG one with two terminal cyanoguanidino groups
- PHMB-GG two terminal guanidine groups
- PHMB-ACG amine-cyanoguanidino
- PHMB-AG amine-guanidino
- GCG guanidine-cyanoguanidino
- a sample of PHMB may comprise a mixture of polymeric biguanides with the three mentioned terminal groups.
- some of the composition can include in-chain polymeric guanide (not shown).
- the subscript "n" represents the average number of repeating groups, and a distribution of polymer length exists for each of the polymers shown below.
- n can be from about 1 to about 50, such as from about 1 to about 20.
- Polyhexamethylene biguanide such as polyhexamethylene biguanide hydrochloride, has a broad antimicrobial range and is fast acting. Further, the antimicrobial agent is stable over a broad pH range.
- the second biocide may comprise a bis-biguanide.
- Bis-biguanide is commonly represented by the following formula, though it is known to exist in other forms.
- a and A 1 each represent either (1 ) a phenyl radical which optionally is substituted by an alkyl or alkoxy group containing from 1 to about 4 carbon atoms, a nitro group, or a halogen atom; (2) an alkyl group containing from 1 to about 12 carbon atoms; or (3) alicyclic groups containing from 4 to about 12 carbon atoms; wherein X and X 1 each represent an alkylene radical containing from 1 to 3 carbon atoms; wherein Z and Z 1 each can be either 0 or 1 ; wherein R and R 1 each represent either hydrogen, or alkyl radical containing from 1 to about 12 carbon atoms, or an aralkyl radical containing from 7 to about 12 carbon atoms; wherein n is an integer from 2 to 12 inclusive; and wherein the chain (CH 2 ) n may optionally be interrupted by oxygen or sulfur atoms, aromatic nuclei, etc.
- the second biocide may comprise chlorhexidine or derivatives or salts thereof. Chlorhexidine is commonly found in the second biocide.
- composition of the present disclosure may include didecyl dimethyl ammonium carbonate and didecyl dimethyl ammonium bicarbonate in combination with a biguanide, such as
- methylglycinediacetic acid tetrasodium ethylenediaminetetraacetic acid, and mixtures thereof.
- the composition of the present disclosure may contain the first biocide in an amount from 2% to 12% by weight, such as from 3% to 8% by weight.
- the composition may contain the second biocide in an amount from 2% to 12% by weight, such as from 3% to 8% by weight.
- the composition of the present disclosure may comprise a first biocide comprising a didecyl dimethyl ammonium carbonate and didecyl dimethyl ammonium bicarbonate, a polyhexamethylene biguanide, an alkalinity builder, a surfactant, and a complexing agent.
- the didecyl dimethyl ammonium carbonate and didecyl dimethyl ammonium bicarbonate may be present in the composition in an amount from about 2% by weight to about 12% by weight.
- the polyhexamethylene biguanide may be present in the composition in an amount from about 2% by weight to about 12% by weight.
- the first and the second biocide can be contained together in a concentrate and later diluted when used.
- the first and second biocide can be present in the concentrate in an amount greater than about 5% by weight, such as in an amount greater than about 10% by weight, such as in an amount greater than about 15% by weight, such as in an amount greater than about 20% by weight.
- the concentrate can contain the first and second biocide in an amount less than about 50% by weight, such as in an amount less than about 30% by weight.
- the anti-microbial composition When used as a hard surface cleaner, the anti-microbial composition can be delivered to a surface to be cleaned, sanitized or disinfected by
- compositions can also be used to sanitize floors, walls, furniture, mirrors, toilet fixtures, windows, and wood surfaces, such as fence rails, porch rails, decks, roofing, siding, window frames, and door frames.
- the compositions, quaternary ammonium chloride compound, and disinfecting active are particularly well suited for application on indirect food contact surfaces, such as cutting boards, utensils, containers, dishes, wash basins, appliances, and countertops.
- the compositions or quaternary ammonium chloride compound can be used to sanitize dairy plant equipment, milking machines, milk pails, tank trucks, and the like. Areas in hospitals would include beds, gurneys, tables, canisters, toilets, waste cans, stands, cabinets, shower stalls, floors, walls or any other non-porous surface.
- water-miscible solvents include ethanol, propanol, benzyl alcohol, phenoxyethanol, isopropanol, diethylene glycol propyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monoisopropyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monobutyl ether, diethylene glycol monoethyl ether, diethylene glycol mono-n-butyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol dibutyl ether, propylene glycol n-butyl ether, tripropylene glycol methyl ether, dipropylene glycol methyl ether, dipropylene glycol butyl ether and combinations thereof.
- Particularly suitable surfactants are alkoxylated alcohol surfactant will generally have between about 2 to about 8 moles of alkoxylation. Typically, there will be between 3 and 6 moles of alkoxylation. One particular example is about 4.5 moles of alkoxylation.
- the alcohol which is alkoxylate will be a Ce- C12 alkyl alcohol. In one embodiment, the alkyl alcohol is a Cs- C10 alkyl alcohol. The alkoxylation may be ethoxylation.
- non-ionic surfactants that may be used in the invention include, but are not limited to, polyoxyethylene glycol alkyl ethers, octaethylene glycol monododecyl ether, pentaethylene glycol monododecyl ether, polyoxypropylene glycol alkyl ethers, glucoside alkyl ethers, decyl glucoside, lauryl glucoside, octyl glucoside, polyoxyethylene glycol octylphenol ethers, polyoxyethylene glycol alkylphenol ethers, glycerol alkyl esters, polyglycerol esters, glyceryl laurate, polyoxyethylene glycol sorbitan alkyl esters, sorbitan alkyl esters,
- Sequestering agents include, for example, acetic acid derivative selected from the group consisting of ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), tetrasodium EDTA.
- EDTA ethylenediaminetetraacetic acid
- NTA nitrilotriacetic acid
- the sequestering agent may also serve to bind other metal ions that may adversely affect the effectiveness of the disinfecting components in the composition.
- sequestering agent may also assist in soil removal and/or preventing soil redeposition into the disinfecting composition while in use.
- the sequestering agents, when present in the concentrate is generally present in an amount up to about 20% by weight, and are typically present in an amount of about 2 to about 8% by weight.
- Suitable pH adjusting agents include sodium hydroxide, sodium citrate and other similar compounds.
- the concentrate and the final disinfectant composition will have a pH in the range of about 6 to about 1 3.
- the disinfectant product may optionally further contain corrosion inhibitors, complexing agents, auxiliaries, preservatives, fragrances, colorants and the like.
- corrosion inhibitors include, for example, organic phosphorous compounds and blend of organic phosphorous compounds with a polymeric component.
- auxiliaries include, for example, polyethylene glycol or other similar compounds. Colorants and fragrances may be added provided they do not interfere with the function of the composition and may serve for identifying the composition.
- the optional further ingredients will make up less than about 20% by weight of the composition.
- the acid is citric acid, phosphoric acid, succinic acid, lactic acid, S,S-ethylenediamine-N,N'-disuccinic acid, 1 -hydroxyethane 1 ,1 - diphosphonic acid (HEDP), dipicolinic acid (DPA), methanesulfonic acid (MSA), their alkaline salts, or any mixture thereof.
- the acid is a mixture of acids.
- the acid comprises one or more of the following organic acids: citric acid, succinic acid, phosphoric acid, and lactic acid.
- the acid comprises one or more of the following acids: citric acid, succinic acid, phosphoric acid, and lactic acid, in combination with another acid.
- citric acid may be used in combination with ethylenediamine-N,N'-disuccinic acid or its alkaline salt, HEDP, and/or MSA.
- succinic acid may be used in combination with ethylenediamine-N,N'-disuccinic acid or its alkaline salt, HEDP, and/or MSA.
- phosphoric acid may be used in combination with ethylenediamine-N,N'-disuccinic acid or its alkaline salt, HEDP, and/or MSA.
- lactic acid may be used in combination with ethylenediamine-N,N'-disuccinic acid or its alkaline salt, HEDP, and/or MSA.
- the composition may include from about 1 % by weight to about 5% by weight of an organic acid such as citric acid, succinic acid, phosphoric acid, lactic acid, or any mixture thereof, in combination with another acid.
- the composition may include from about 1 % by weight to about 5% by weight of an organic acid such as citric acid, succinic acid, phosphoric acid, lactic acid, or any mixture thereof, in combination with from about 0.05% by weight to about 5% by weight of another acid.
- the composition may include from about 2% by weight to about 4% by weight of an organic acid such as citric acid, succinic acid, phosphoric acid, lactic acid, or any mixture thereof, in combination with from about 0.1 % by weight to about 4% by weight of another acid such as ethylenediamine-N,N'-disuccinic acid or its alkaline salt, HEDP, and/or MSA.
- an organic acid such as citric acid, succinic acid, phosphoric acid, lactic acid, or any mixture thereof
- another acid such as ethylenediamine-N,N'-disuccinic acid or its alkaline salt, HEDP, and/or MSA.
- the wipe is a single use wipe that is impregnated with the disinfecting composition and is stored in a container that will dispense the wipe to a user.
- the container with the wipes may contain a single wipe, or several wipes.
- Suitable containers include a pouch containing a single wipe, such as a moist towelette which is torn open by the user, or may be a pouch with a resealable opening containing several wipes in a stacked fashion, a rolled fashion or other suitable formation that would allow a single wipe to be removed from the opening at a time.
- Pouches are generally prepared form a fluid impervious material, such as a film, a coated paper or foil or other similar fluid impervious materials.
- a fluid impervious container having an opening to access the wipes in the container.
- Containers may be molded plastic container with lids that are fluid impervious. Generally, the lid will have an opening to access the wipes in the container.
- the wipe in the container may be in a interleaved stacked, such that as a wipe is removed from the container the next wipe is positioned in the opening of the container ready for the user to remove the next wipe.
- the wipe may be a continuous material which is perforated between the individual wipes of the continuous material.
- continuous wipe material with perforations may be in a folded form or may be in a rolled form.
- the wipe material is feed from the center of the rolled material.
- the next wipe is positioned in the opening for the use to remove the next wipe, when needed.
- Disposable wipes provide advantages over other application vehicles, such as a reusable sponge, rag or the like. Unlike sponges, rags and the like, which are used repeatedly, the impregnated wipe is used a single time and disposed of. As is mentioned above, reused sponge or rag presents problems since the sponge or rags may carry microbes that are not easily killed by the disinfecting composition. Further, the disinfecting composition is formulated to treat hard surface, not porous soft surfaces that are present in sponges or rags.
- the disinfecting composition can be impregnated into the wipe such that the wipe is pre-moistened and will express or release the disinfecting composition on to the surface as the wipe is run across the surface to be treated. Generally, the disinfecting composition is saturated into the wipe such that the wipe will release the disinfecting composition to the surface through the wiping action.
- Suitable wipe substrates include woven and nonwoven materials.
- nonwoven web material may be used.
- exemplary nonwoven materials may include, but are not limited to meltblown, coform, spunbond, airlaid, hydroentangled nonwovens, spunlace, bonded carded webs, and laminates thereof.
- the nonwoven may be laminated with a film material as well.
- the fibers used to prepare the wipe substrate may be cellulosic fiber,
- the wipe is impregnated with a liquid component containing both active and inert ingredients within the allowable tolerance levels and the disinfecting composition expressed from the wipe contains active ingredients within the allowable tolerance levels.
- the antimicrobial disinfecting composition is allowed to remain on the surface for a period of time.
- the antimicrobial composition may be applied to the surface and allowed to dry or may alternatively be dried by wiping the surface with a dry wipe or wiping device, which is preferably unused.
- the disinfectant composition may be used as a hand sanitizer.
- the biocides of the present disclosure can be combined with any of the ingredients described above.
- the biocides may be combined with a solvent, such as water and/or an alcohol.
- a foaming agent may be added that causes the composition to foam when pumped from a dispenser.
- the foaming agent may comprise any suitable foaming agent that is compatible with the biocides.
- the foaming agent may comprise a dimethicone.
- isophthalaldehyde terephthalaldehyde, or combinations thereof.
- the structures of the phthalaldehyde isomers are shown below:
- the preferred aromatic dialdehyde is OPA.
- the disinfectant composition may be used for disinfection of instruments, such as for pre-cleaning and disinfection or for terminal, high-level disinfection of a device, medical instrument or endoscope.
- the disinfectant composition could be applied by immersing the instrument in the appropriate concentration of the disinfectant composition.
- plastic or metal containers, stainless steel sinks, or any other suitable container may be used as a vessel to hold the disinfectant composition.
- complete immersion of the instrument or device or endoscope including voids, lumens and hollow sections, may be necessary.
- the channels of the endoscope and other instruments may need to be flushed. In general, after disinfection the instrument must be rinsed and flushed thoroughly with water, preferably with significant quantities of water.
- the appropriate concentration of the disinfectant composition may be from about 500 mg/L to about 25,000 mg/L, such as from about 1 ,000 mg/L to about 23,000 mg/L.
- the preferred concentration of the disinfectant composition may be from about 500 mg/L to about 10,000 mg/L, such as from about 1 ,000 mg/L to about 9,000 mg/L, such as from about 2,000 mg/L to about 8,000 mg/L, such as from about 3,000 mg/L to about 7,000 mg/L, such as from about 4,000 mg/L to about 6,000 mg/L.
- the preferred disinfectant composition concentration may be from about 5,000 mg/L to about 25,000 mg/L, such as from about 8,000 to about 23,000 mg/L, such as from about 10,000 to about 20,000 mg/L.
- the necessary contact time may range from about 10 minutes to about 60 minutes, preferably from about 15 minutes to about 30 minutes. The necessary contact time may be adjusted based on the targeted disinfection level.
- the disinfectant composition may be used for the disinfection of instruments in an automated washer-disinfector.
- the biocides When used as a preservative, the biocides may be combined with any suitable surfactant.
- the surfactant for instance, may comprise an anionic surfactant.
- Suitable anionic surfactants having a sulfate moiety include sulfates represented by the formula RS0 4 M, wherein R is a chain containing from about 10 to about 18 atoms at the backbone of the chain, M is a cation such as ammonium; alkanolamines, such as triethanolamine; monovalent metals, such as sodium and potassium; and polyvalent metals, such as magnesium, and calcium.
- the anionic surfactants having a sulfate moiety are alkyl sulfates wherein R is an alkyl having from 10 to 18 carbon atoms, preferably from 10 to 16 carbon atoms, more preferably from 10 to 14 carbon atoms.
- R can be a straight or branched chain.
- R is a straight chain.
- R is an octyl group.
- Exemplary alkyl sulfates include sodium dodecyl sulfate, potassium dodecyl sulfate, triethylamine dodecyl sulfate, triethanolamine dodecyl sulfate, monoethanolamine dodecyl sulfate, diethanolamine dodecyl sulfate and
- Suitable anionic surfactants having a sulfonate moiety include sulfonates having the formula RSO 3 M, wherein R is a straight or branch chain containing 10 to 18 atoms at the backbone of the chain, M is a cation such as ammonium;
- Exemplary sulfonates suitable for the composition of the invention includes sodium dioctyl sulphosuccinate, and primary and secondary alkyl sulphonates.
- R is an alkyl having from about 10 to about 18, preferably from 10 to 16, more preferably from 10 to 14 carbon atoms. In one embodiment, R is a C12 alkyl group.
- the product When incorporated into a personal care product, the product may contain an emulsifier, a consistency factor, an emollient, and/or an active ingredient.
- Suitable emulsifiers are e.g. anionics as salts of fatty acids e.g. sodium stearate or sodium palmitate, organic soaps e.g. mono- di- or triethanolaminoeate, sulfated or sulfonated compounds e.g. sodium lauryl sulfate or sodium cetyl sulfonate, saponines, lamepones; cationics as quaternary ammonium salts;
- nonionics as fatty alcohols, fatty acid ester with saturated or unsaturated fatty acids, polyoxyethylenesters or polyoxyethylenethers of fatty acids, polymers from ethylene oxide and propylene oxide or propylene glycol, amphotherics as phosphatides, proteins as gelatine, casein alkylamidobetaines, alkyl betaines and amphoglycinates, alkyl phosphates, alkylpolyoxyethylene phoaphates or the corresponding acids, silicone derivatives, e.g. alkyl dimethiconecoplyol.
- dimethicone laureth-23, laureth-4, polydecene, retinyl palmitate, quaternized protein hydrolysates, quaternized cellulose and starch derivatives, quaternized copolymers of acrylic or methacrylic acid or salts, quaternized silicone derivatives.
- Suitable emollients are e.g. cetearyl isononanoate, cetearyl octanoate, decyl oleate, isooctyl stearate, coco caprylate/caprate, ethylhexyl hydroxystearate, ethylhexyl isononanoate, isopropyl isostearate, isopropyl myristate, oleyl oleate, hexyl laurate, paraffinum liquidum, PEG-75 lanolin, PEG-7 glyceryl cocoate, petrolatum, ozokerite cyclomethicone, dimethicone, dimethicone copolyol, dicaprylyl ether, butyrospermum parkii, buxus chinensis, canola, carnauba cera, copernicia cerifera, Oenothera biennis, ela
- compositions may further contain active ingredients, e.g. antimicrobials, anti-inflammatories, plant extracts, bisabolol, panthenol, tocopherol, actives for anti-stinging, anti-irritant or anti-dandruff applications, or anti-aging agents such as retinol, melibiose and the like.
- active ingredients e.g. antimicrobials, anti-inflammatories, plant extracts, bisabolol, panthenol, tocopherol, actives for anti-stinging, anti-irritant or anti-dandruff applications, or anti-aging agents such as retinol, melibiose and the like.
- active ingredients e.g. antimicrobials, anti-inflammatories, plant extracts, bisabolol, panthenol, tocopherol, actives for anti-stinging, anti-irritant or anti-dandruff applications, or anti-aging agents such as retinol, mel
- Medicago officinalis Actinidia chinensis, allantoin, Aloe barbadensis, Anona cherimolia, Anthemis nobilis, Arachis hypogaea, Arnica Montana, Avena sativa, beta-carotene, bisabolol, Borago officinalis, butylenes glycol, Calendula officinalis, Camellia sinensis, camphor, Candida bombicola, capryloyl glycine, Carica papaya, Centaurea cyanus, cetylpyridinium chloride, Chamomilla recutita, Chenopodium quinoa, Chinchona succirubra, Chondrus crispus, Citrus aurantium dulcis, Citrus grandis, Citrus limonum, Cocos nucifera, Coffea Arabica, Crataegus monogina, Cucumis melo, dichlorophenyl imidazoldioxolan,
- Bacteria were maintained on nutrient agar and fungi on malt agar or a spore suspension in physiological saline (0.85% (w/v) NaCI).
- MIC Minimum Inhibitory Concentration
- FIC Concentration Biocide A attributable to antimicrobial
- a synergistic interaction is the total effect of two chemicals being greater than their effects individually. In relation to disinfection, this means that a pair of synergistic biocides will have greater antimicrobial activity in the presence of each other against certain microorganisms in comparison to only a single biocide being present.
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Abstract
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
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JP2018567667A JP7026060B2 (en) | 2016-06-24 | 2017-06-19 | Synergistic combination of biocides |
US16/310,871 US20200305435A1 (en) | 2016-06-24 | 2017-06-19 | Synergistic combination of biocides |
CN201780050916.XA CN109640656A (en) | 2016-06-24 | 2017-06-19 | The synergistic combination of biocide |
BR112018076819-7A BR112018076819A2 (en) | 2016-06-24 | 2017-06-19 | synergistic combination of biocides |
EP17734912.3A EP3457850A1 (en) | 2016-06-24 | 2017-06-19 | Synergistic combination of biocides |
JP2021197945A JP7442491B2 (en) | 2016-06-24 | 2021-12-06 | Synergistic combination of biocides |
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US201662354489P | 2016-06-24 | 2016-06-24 | |
US62/354,489 | 2016-06-24 |
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PCT/US2017/038101 WO2017222965A1 (en) | 2016-06-24 | 2017-06-19 | Synergistic combination of biocides |
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US (1) | US20200305435A1 (en) |
EP (1) | EP3457850A1 (en) |
JP (2) | JP7026060B2 (en) |
CN (1) | CN109640656A (en) |
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WO (1) | WO2017222965A1 (en) |
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WO2019036637A1 (en) * | 2017-08-18 | 2019-02-21 | Lonza Inc. | Premoistened wipes with virucidal properties against non-enveloped viruses |
CN112055538A (en) * | 2018-05-31 | 2020-12-08 | Vb日本技术株式会社 | Antibacterial and antiviral composition and aqueous solution |
US10952430B2 (en) | 2019-02-06 | 2021-03-23 | Virox Technologies Inc. | Shelf-stable antimicrobial compositions |
WO2021245208A1 (en) * | 2020-06-03 | 2021-12-09 | JVS Products Limited | Compositions |
WO2022016069A1 (en) * | 2020-07-17 | 2022-01-20 | Sterilex, Llc | Disinfectant/sanitizer solutions |
EP3949733A1 (en) * | 2020-08-06 | 2022-02-09 | JVS Products Limited | Disinfectant compositions |
WO2022038351A1 (en) * | 2020-08-17 | 2022-02-24 | Helperby Therapeutics Limited | Disinfectant composition |
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CN111642512A (en) * | 2020-03-12 | 2020-09-11 | 天天向上(宁波)医疗科技有限公司 | High-efficiency disinfectant and preparation method and use method thereof |
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WO2023097416A1 (en) * | 2021-11-30 | 2023-06-08 | Ecolab Usa Inc. | A residual sanitizer used for hard surface residual sanitization |
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- 2017-06-19 WO PCT/US2017/038101 patent/WO2017222965A1/en unknown
- 2017-06-19 CN CN201780050916.XA patent/CN109640656A/en active Pending
- 2017-06-19 EP EP17734912.3A patent/EP3457850A1/en active Pending
- 2017-06-19 BR BR112018076819-7A patent/BR112018076819A2/en not_active Application Discontinuation
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Also Published As
Publication number | Publication date |
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JP2022037055A (en) | 2022-03-08 |
JP7442491B2 (en) | 2024-03-04 |
BR112018076819A2 (en) | 2019-04-02 |
US20200305435A1 (en) | 2020-10-01 |
CN109640656A (en) | 2019-04-16 |
EP3457850A1 (en) | 2019-03-27 |
JP7026060B2 (en) | 2022-02-25 |
JP2019520362A (en) | 2019-07-18 |
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